Product Description Product website: http://www.finerchem.com Product Name 4-Isopropylphenol CAS No. 99-89-8
Cas:99-89-8
Min.Order:1 Gram
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Cas:99-89-8
Min.Order:100 Gram
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Cas:99-89-8
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inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
Hangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
Cas:99-89-8
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inquiryJ&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
Massive Chemical is certified with ISO9001 and ISO14001 manufacturer for this product. We will offer all documents as requirement for the materials which includes, Certificate of Analysis, Material Safety Data Sheet, and Method of Analysis and
Cas:99-89-8
Min.Order:1 Gram
FOB Price: $1.0
Type:Lab/Research institutions
inquiryProduct Details Grade: pharmaceutical grade Purity:99%+ ProductionCapacity: 1000 Kilogram/Month Scope of use: For scientific research only(The product must be used legally) Our Advantage 1. Best quality with competitive price. 2. Quick shipping,
Cas:99-89-8
Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
R & D enterprises have their own stock in stockAppearance:To be subject to the object Package:Customized Application:pharmaceutical intermediates Transportation:Air Port:Shanghai;Guangzhou
high purity,in stock Package:25kg/drum,or as per customers'demand Application:API,Pharmaceutical intermediates Transportation:air,sea,courier
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high quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
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Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:99-89-8
Min.Order:1 Kilogram
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Phenol,4-(1-methylethyl)- Application:Organic Chemicals
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Known for its best quality and competitve price, this chemicals we offered is widely appreciated by our customers. Prompt reaction, good quality and best service make us reliable and outstanding in this industry.Appearance:Off white crystal Storage:k
Cas:99-89-8
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inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:any port in China
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Cas:99-89-8
Min.Order:10 Milligram
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Type:Lab/Research institutions
inquiry4-Isopropylphenol CAS#99-89-8 1.in very competitive price 2.Quality Guaranteed 3.Fast delivery Appearance:white crystalline powder Storage:Keep in a cool, dry, dark location in a tightly sealed container or cylinder Package:25kg/drum or as
HENAN SUNLAKE ENTERPRISE CORPORATION Our company advantages: 1、The highest quality with the competitive price. 2、Professional human services. 3、The fastest and safest delivery service. 4、The faster and safest delivery service. 5、The hig
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Cas:99-89-8
Min.Order:1 Kilogram
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inquiryBefore-Sale Service:---Any inquiries will be replied within 12 hours.---Golden Manufactory under?ISO/GMP?with?large stock.---Dedication to quality,We?have?strict?quality?control?system.?---OEM/ODM Available.---Sample is available for your evaluation
Cas:99-89-8
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inquiryConditions | Yield |
---|---|
With 1-n-butyl-3-methylimidazolim bromide at 200 - 220℃; for 0.5h; Microwave irradiation; Inert atmosphere; | 99% |
With hydrogen iodide |
Conditions | Yield |
---|---|
With 1-n-butyl-3-methylimidazolim bromide at 220℃; for 0.666667h; Inert atmosphere; Microwave irradiation; | 98% |
With trimethylsilyl iodide at 105 - 114℃; for 0.25h; Microwave irradiation; Inert atmosphere; | 92% |
With tetrachlorosilane; borontrifluoride acetic acid; lithium iodide In toluene; acetonitrile at 70℃; for 10h; | 89% |
With hydrogen iodide |
Conditions | Yield |
---|---|
With ammonium bicarbonate In water at 20℃; for 2h; Schlenk technique; | 97% |
(4-isopropylphenoxy)trimethylsilane
4-Isopropylphenol
Conditions | Yield |
---|---|
With methanol; 1,3-disulfonic acid imidazolium hydrogen sulfate at 20℃; for 0.0666667h; Green chemistry; | 96% |
With poly (ethylene glycol)-sulfonated sodium montmorillonite nanocomposite In methanol at 20℃; for 0.166667h; | 91% |
4-propoxycumene
4-Isopropylphenol
Conditions | Yield |
---|---|
With 1-n-butyl-3-methylimidazolim bromide at 200 - 220℃; for 0.5h; Microwave irradiation; Inert atmosphere; | 96% |
(4-isopropylphenyl)boronic acid
4-Isopropylphenol
Conditions | Yield |
---|---|
With dihydrogen peroxide In ethanol at 20℃; for 0.166667h; | 96% |
With iron(III) oxide; oxygen In tetrahydrofuran Irradiation; | 95% |
With iron(III) oxide; oxygen In tetrahydrofuran at 20℃; Irradiation; | 95% |
[2-(4-isopropylphenoxy)ethyl]trimethylsilane
4-Isopropylphenol
Conditions | Yield |
---|---|
Stage #1: [2-(4-isopropylphenoxy)ethyl]trimethylsilane With cesium fluoride In N,N-dimethyl-formamide at 60℃; for 1h; Inert atmosphere; Stage #2: With water In N,N-dimethyl-formamide Inert atmosphere; | 88% |
4-isopropylphenyl lithium
4-Isopropylphenol
Conditions | Yield |
---|---|
With titanium(IV) isopropylate; tert.-butylhydroperoxide In diethyl ether at -78℃; for 12h; | 80% |
4-Isopropylphenol
Conditions | Yield |
---|---|
With sodium hydride; bis(pinacol)diborane In 1,2-dichloro-ethane at 70℃; for 12h; Inert atmosphere; | 77% |
Conditions | Yield |
---|---|
Stage #1: (1R,5R)-(+)-β-pinene With ozone In methanol Stage #2: With iron(III) chloride hexahydrate In methanol at 60℃; for 2h; | A 15% B 70% |
(-)-menthol
phenol
A
2-(1-methylethyl)phenol
B
4-Isopropylphenol
C
isopropoxybenzene
D
3-isopropylhydroxybenzene
Conditions | Yield |
---|---|
at 120℃; for 15h; | A 64% B 23% C 10% D 3% |
Conditions | Yield |
---|---|
Stage #1: 1,4-bis(1-methylethyl)benzene With N-hydroxyphthalimide; 2,2'-azobis(isobutyronitrile); oxygen In acetonitrile at 75℃; under 760.051 Torr; for 20h; Stage #2: With sulfuric acid In acetonitrile at 75℃; for 4h; Further stages.; | A 33% B 61% |
isopropyl alcohol
phenol
A
2-(1-methylethyl)phenol
B
4-Isopropylphenol
C
5-propylphenol
D
2,6-diisopropylphenol
Conditions | Yield |
---|---|
With supercritical water at 399.84℃; for 1h; Kinetics; Further Variations:; Time; | A 57.9% B 2.4% C 6.9% D 5.9% |
A
4-Isopropylphenol
B
1-(allyloxy)-4-isopropylbenzene
C
2-allyl-4-isopropylphenol
Conditions | Yield |
---|---|
With tetrakis(triphenylphosphine) palladium(0) In toluene at 110℃; for 0.5h; Inert atmosphere; | A 44% B 8% C 48% |
isopropyl alcohol
phenol
A
2-(1-methylethyl)phenol
B
4-Isopropylphenol
C
2,6-diisopropylphenol
D
isopropoxybenzene
Conditions | Yield |
---|---|
With HMCM-49/MCM-41 composite at 180℃; under 760.051 Torr; for 1h; Flow reactor; | A 41.6% B 13.3% C n/a D n/a |
(-)-menthol
phenol
A
2-(1-methylethyl)phenol
B
4-Isopropylphenol
C
3-isopropylhydroxybenzene
Conditions | Yield |
---|---|
at 160℃; for 15h; | A 37% B 26% C 37% |
isopropyl alcohol
phenol
A
2-(1-methylethyl)phenol
B
4-Isopropylphenol
C
2,6-diisopropylphenol
D
2,4,6-triisopropylphenol
Conditions | Yield |
---|---|
With HMCM-49 at 180℃; under 760.051 Torr; for 1h; Flow reactor; | A 35.5% B 9.4% C n/a D n/a |
(4-isopropylbenzyl)trimethylsilane
4-Isopropylphenol
Conditions | Yield |
---|---|
With sodium persulfate; oxygen In acetonitrile at 55℃; for 20h; | 33% |
Isopropylbenzene
A
2-(1-methylethyl)phenol
B
4-Isopropylphenol
C
1-methyl-1-phenylethyl alcohol
D
3-isopropylhydroxybenzene
Conditions | Yield |
---|---|
With pyridine-2-carbaldehyde; 2-(Aminomethyl)pyridine; iron(II) trifluoromethanesulfonate acetonitrile disolvate; dihydrogen peroxide In acetonitrile at 25℃; for 1.5h; chemoselective reaction; | A 7% B n/a C 6% D n/a |
With VO(O2)(picolinato)(H2O)2 In acetonitrile at 20℃; Product distribution; Mechanism; |
Conditions | Yield |
---|---|
bei der Destillation; | |
With palladium on activated charcoal | |
With copper oxide-chromium oxide; hydrogen at 220 - 230℃; under 132391 Torr; |
Conditions | Yield |
---|---|
Hydrogenolyse; | |
at 160℃; under 7600 - 15200 Torr; Hydrogenation.in Gegenwart eines wismuthaltigen Nickel-, Kobalt- oder Kupfer-Katalysators; |
Conditions | Yield |
---|---|
With dihydroxodifluoroboric acid bei Siedetemperatur; | |
With aluminium trichloride |
Conditions | Yield |
---|---|
With sulfuric acid; sodium nitrite Erwaermen der erhaltenen Diazoniumsalz-Loesung auf 50-60grad; | |
via p-cumenediazonium salt; Multistep reaction; | |
With sulfuric acid; sodium nitrite Erwaermen der erhaltenen Diazoniumsalz-Loesung auf 50-60grad; |
2-hydroxy-5-isopropylbenzoic acid
4-Isopropylphenol
Conditions | Yield |
---|---|
With hydrogenchloride at 180℃; |
Conditions | Yield |
---|---|
With sulfuric acid | |
With sulfuric acid |
Conditions | Yield |
---|---|
With aluminium trichloride anschliessendes Behandeln mit H2O; |
isopropyl alcohol
phenol
A
2-(1-methylethyl)phenol
B
4-Isopropylphenol
Conditions | Yield |
---|---|
With phosphoric acid at 95 - 130℃; | |
With iron(III) chloride at 120 - 130℃; | |
With boron trifluoride |
Conditions | Yield |
---|---|
With boron trifluoride | |
With aluminium trichloride; Petroleum ether at 110 - 120℃; | |
With iron(III) chloride at 120 - 130℃; |
Conditions | Yield |
---|---|
With hydrogenation catalyst at 220 - 230℃; |
Conditions | Yield |
---|---|
With boron trifluoride | |
With phosphoric acid at 95 - 130℃; | |
With boric acid Erhitzen des Reaktionsprodukts mit wenig H2SO4 und anschliessend mit H2O; |
Conditions | Yield |
---|---|
With caesium carbonate In acetonitrile | 100% |
With potassium carbonate In N,N-dimethyl-formamide at 0 - 20℃; Inert atmosphere; | 92% |
With potassium carbonate In acetone for 4h; Reflux; | 80.3% |
Conditions | Yield |
---|---|
With potassium carbonate In acetone for 12h; Reflux; Sealed tube; | 100% |
Stage #1: 4-Isopropylphenol With potassium carbonate In N,N-dimethyl-formamide for 2h; Inert atmosphere; Stage #2: benzyl bromide In N,N-dimethyl-formamide at 60℃; for 12h; | |
With tetra-(n-butyl)ammonium iodide; potassium hydroxide In acetonitrile for 2h; | |
With tetra-(n-butyl)ammonium iodide; potassium hydroxide In acetonitrile for 1h; Cooling; |
2-chloro-5-nitropyridine
4-Isopropylphenol
2-(4-isopropylphenoxy)-5-nitropyridine
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 24h; | 99% |
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 24h; | 99% |
With sodium hydroxide; tetrabutyl-ammonium chloride In water; benzene at 56℃; for 0.25h; | 71% |
4-Isopropylphenol
thianthrene cation radical perchlorate
Conditions | Yield |
---|---|
In acetonitrile for 18h; | 99% |
4-Isopropylphenol
Phenyl glycidyl ether
1-(4'-isopropylphenoxy)-3-phenoxypropan-2-ol
Conditions | Yield |
---|---|
With 2-tert-butylimino-2-diethylamino-1,3-dimethylperhydro-1,3,2-diazaphosphorine supported on polystyrene (PS-BEMP; PS = 200-400 mesh polystyryl with 2percent of divinylbenzene) at 60℃; for 18h; Neat (no solvent); regioselective reaction; | 99% |
With 1,4-bis(4-vinylphenoxy)benzene crosslinked polystyrene functionalized with 1,5,7-triazabicyclo[4.4.0]dec-5-ene In neat (no solvent) at 60℃; for 18h; Reagent/catalyst; Green chemistry; |
4-Isopropylphenol
2-cyano-1-phenylacetylene
(Z)-3-(4-isopropylphenoxy)-3-phenylacrylonitrile
Conditions | Yield |
---|---|
With sodium carbonate In N,N-dimethyl-formamide at 20 - 25℃; for 12h; optical yield given as %de; | 99% |
Conditions | Yield |
---|---|
With caesium carbonate In N,N-dimethyl-formamide at 80℃; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
With hydrogen In dodecane at 200℃; under 15001.5 Torr; for 2h; | 98.2% |
Conditions | Yield |
---|---|
With potassium carbonate In acetone Heating; | 98% |
Stage #1: 4-Isopropylphenol With potassium carbonate In acetone Stage #2: methyl iodide In acetone Further stages.; | 98% |
With sodium hexamethyldisilazane In tetrahydrofuran at 20℃; for 23h; Inert atmosphere; | 83% |
4-Isopropylphenol
2-iodo-4-(1-methylethyl)phenol
Conditions | Yield |
---|---|
With N-iodo-succinimide; toluene-4-sulfonic acid In dichloromethane at 20℃; | 98% |
Stage #1: 4-Isopropylphenol With ammonium iodide In methanol at 0℃; for 0.0333333h; Stage #2: With potassium phosphate In methanol for 0.0833333h; | 90% |
With N-iodo-succinimide In various solvent(s) at 27℃; for 0.666667h; | 89% |
4-Isopropylphenol
1,1,1,3,3,3-hexamethyl-disilazane
(4-isopropylphenoxy)trimethylsilane
Conditions | Yield |
---|---|
With 3-methyl-1-sulfonic acid imidazolium hydrogen sulfate at 20℃; for 0.0333333h; Neat (no solvent); | 98% |
With succinimide-N-sulfonic acid In acetonitrile at 20℃; for 0.0333333h; chemoselective reaction; | 98% |
With 1,3-disulfonic acid imidazolium hydrogen sulfate In neat (no solvent) at 20℃; for 0.0333333h; Green chemistry; | 98% |
4-Isopropylphenol
ortho-nitrofluorobenzene
1-(4-isopropylphenoxy)-2-nitrobenzene
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 90℃; for 3h; Inert atmosphere; | 98% |
Stage #1: 4-Isopropylphenol With potassium tert-butylate In tetrahydrofuran for 1h; Stage #2: ortho-nitrofluorobenzene In tetrahydrofuran |
4-Isopropylphenol
ethyl bromoacetate
(4-isopropylphenyl)acetic acid ethyl ester
Conditions | Yield |
---|---|
With potassium carbonate In DMF (N,N-dimethyl-formamide) at 20℃; for 48h; | 98% |
4-Isopropylphenol
(E)-1-Bromo-2-butene
(E)-1-(but-2-en-1-yloxy)-4-isopropylbenzene
Conditions | Yield |
---|---|
With potassium carbonate In acetone for 6h; Heating; | 97% |
4-Isopropylphenol
C18H20O3
Conditions | Yield |
---|---|
With tetrakis(actonitrile)copper(I) hexafluorophosphate; N,N'-di-tert-butylethylenediamine; oxygen In dichloromethane at 20 - 23℃; under 760.051 Torr; for 4h; | 97% |
With tetrakis(actonitrile)copper(I) hexafluorophosphate; N,N'-di-tert-butylethylenediamine; oxygen In dichloromethane at 23℃; under 760.051 Torr; for 4h; Reagent/catalyst; | 92% |
With N,N'-di-tert-butylethylenediamine; oxygen; copper(II) acetate monohydrate In dichloromethane at 25℃; under 1520.1 Torr; for 4h; Catalytic behavior; Glovebox; | 87% |
4-Isopropylphenol
2-(diethylamino)ethyl chloride
1-(2-Diethylaminoethoxy)-4-isopropyl-benzol
Conditions | Yield |
---|---|
96% |
4-Isopropylphenol
Conditions | Yield |
---|---|
With palladium diacetate; tert-butyl XPhos In toluene at 100 - 110℃; for 7h; Inert atmosphere; | 96% |
Conditions | Yield |
---|---|
With nitric acid; copper(II) nitrate In water at 20 - 25℃; for 2h; | 95.1% |
With Eu-Mo-modified montmorillonite HKSF; nitric acid In tetrahydrofuran at 20℃; for 12h; | 87% |
With nitrourea; silica-gel-supported sulfuric acid In dichloromethane at 20℃; for 3.83333h; regioselective reaction; | 77% |
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 110℃; for 14h; Alkylation; | 95% |
Conditions | Yield |
---|---|
With rice husk ash at 80℃; for 0.25h; Green chemistry; | 95% |
With rice-husk-supported FeCl3 nano particles In neat (no solvent) at 80℃; for 1h; | 93% |
With H3[P(Mo3O10)4]*nH2O at 20℃; for 0.05h; | 87% |
Conditions | Yield |
---|---|
With triethylamine; magnesium chloride In acetonitrile at 70℃; for 2h; | 95% |
With magnesia In neat (no solvent) for 0.283333h; Microwave irradiation; regioselective reaction; | 75% |
With triethylamine; magnesium chloride In tetrahydrofuran for 6h; Reflux; | 75% |
Conditions | Yield |
---|---|
With sulfuric acid; acetic acid at 40℃; for 24h; Inert atmosphere; | 95% |
With sulfuric acid at 20℃; for 1h; Inert atmosphere; | 42% |
Conditions | Yield |
---|---|
With copper(l) iodide; caesium carbonate In 1-methyl-pyrrolidin-2-one at 160℃; for 24h; Inert atmosphere; Schlenk technique; | 95% |
4-Isopropylphenol
iodobenzene
carbon monoxide
4-isopropylphenyl benzoate
Conditions | Yield |
---|---|
With dicarbonyl(acetylacotonato)rhodium(I); triethylamine; 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene In toluene at 120℃; for 48h; Inert atmosphere; Autoclave; Schlenk technique; | 95% |
With palladium diacetate; potassium carbonate at 100℃; under 5250.53 Torr; for 3h; Catalytic behavior; | 50 %Chromat. |
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